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EC number: 216-721-0 | CAS number: 1653-19-6
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Endpoint summary
Administrative data
Description of key information
Although an investigation of skin corrosivity and irritation in which rabbits were treated topically with 2,3 dichloro-1,3 butadiene in a 50/50 mixture with methylene chloride did not indicate the substance to be corrosive or an irritant, the study did not provide sufficient information to determine the potential dermal irritation elicited by skin contact. On the basis of limited information on the ocular irritancy of 2,3 dichloro-1,3 butadiene provided in the OECD SIDS Initial Assessment Report, 2,3 dichloro-1,3 butadiene can be regarded as a potential eye irritant. There are no substantive data from guideline compliant studies or other evidence to indicate that DCBD is a potential skin or respiratory irritant.
Key value for chemical safety assessment
Skin irritation / corrosion
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Eye irritation
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Additional information
In a non-standard study of irritation and corrosivity in which six albino rabbits received topical applications (on skin clipped free of hair on their backs) of 2,3 dichloro-1,3 butadiene /methylene chloride (50/50) no reactions indicative of dermal corrosion or irritation were reported. The study did not provide sufficient information to determine the potential dermal irritation elicited by skin contact with 2,3 dichloro-1,3 butadiene.
Two in vivo studies on the potential ocular irritancy of DCBD have been evaluated by the OECD as part of ICCA HPV initiative (SIDS Initial Assessment Report 2006). Khechumov et al., (1972) reported that inflammation and purulent conjunctivitis were observed in rabbits after drops of 2,3 dichloro-1,3 butadiene (unspecified isomer of unknown purity) were placed in their conjunctival sac. The conjunctivitis was reversible within 21-22 days. Marhold (1986) reported that the application of 500 mg 2,3 dichloro-1,3 butadiene (unknown purity) into the eyes of rabbits for 24 hours lead to a mild eye irritation (Marhold, 1986). In a precautionary approach, on the basis of limited information on the ocular irritancy of DCBD provided in the OECD SIDS Initial Assessment Report, 2,3 dichloro-1,3 butadiene can be regarded as a potential eye irritant.
Respiratory irritation, characterised by degeneration of the nasal olfactory epithelium, has been reported in rats following sub-chronic whole body inhalation exposures to 2,3 dichloro-1,3 butadiene at concentrations up to 50 ppm. These effects have not however been confirmed by acute or single administration guideline-compliant studies.
Effects on skin irritation/corrosion: irritating
Effects on eye irritation: irritating
Effects on respiratory irritation: irritating
Justification for classification or non-classification
On the basis of limited information on the ocular irritancy provided in the OECD SIDS Initial Assessment Report, 2,3 dichloro-1,3 butadiene can be regarded as an eye irritant. GHS classification is proposed as: Eye Irrit. 2; H319: Causes serious eye irritation (67/548/EEC self classification: Xi; R36 Irritant; Irritating to eyes)
In limited studies, 2,3 dichloro-1,3 butadiene administered with methylene chloride (50:50) was not found to be dermal corrosive and no indications of skin irritation were observed. Data from unreliable studies suggest, that 2,3 -dichloro-1,3 -butadiene is irritating to the skin of rabbits. Therefore a classification as Xi, R 38, GHS: skin Irrit. 2, H315: causes skin irritation is proposed.
Although indications of respiratory tract irritation have been reported in a sub-chronic, whole body inhalation exposure study in rats, this has not been confirmed by acute or single administration studies conducted according to the relevant guidelines for respiratory irritation. Although no clear evidence for respiratory irritation is obvious, a respiratory tract irritation cannot be excluded and therefore a classification as Xi, R 37, GHS: STOT Single Exp. 3, H335: May cause respiratory irritation is proposed.
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